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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235823Generated: October 27, 2026

4-(4-Aminophenyl)butanoic acid → 4-[4-(2-Methyl-3,5-diphenyl-pyrrol-1-yl)-phenyl]-butyric acid

https://huagongshe.com/reaction/2235823

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Aminophenyl)butanoic acidHCID 27049—
Reactant1,3-Diphenylpentane-1,4-dioneHCID 13184731—
SolventAcetic AcidHCID 176—
Product4-[4-(2-Methyl-3,5-diphenyl-pyrrol-1-yl)-phenyl]-butyric acidHCID 24797469—

Reaction Steps

A soln of 1,3-diphenyl-pentane-1,4-dione (104 mg; 0.412 mmol) and 4-(4-amino-phenyl)-butyric acid (89 mg; 0.497 mmol) in acetic acid (2 mL) was heated at 120° C. After 6 h, the reaction was concentrated on a rotary evaporator. Ethyl acetate (5 mL) was added and this washed with H2O (1×2 mL) and satd NaCl (1×3 mL). The organic portion was dried (MgSO4) and filtered through silica with an EtOAc wash. Crude product was adsorbed onto silica (0.3 g) then purified by MPLC (12 g of silica using a 0→50% EtOAc in hexanes gradient). Pure product was obtained as a white solid (115 mg; 71%). 1H NMR (CDCl3) δ 7.54-7.49 (m, 2H), 7.44-7.38 (m, 2H), 7.26-7.07 (m, 10H), 6.56 (s, 1H), 2.72 (t, J=7.6 Hz, 2H), 2.40 (t, J=7.4 Hz, 2H), 2.25 (s, 3H), 2.00 (m, 2H); LC-MS (ESI−) 394 ([M−H]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714022B2
Source datasetuspto-grants-2010_05
ORD IDord-1be8b1e2984040019704f78488e1b97c
Source noteuspto-grants-2010_05